CmlI N-Oxygenase Catalyzes the Final Three Steps in

Aug 20, 2017 - CmlI catalyzes the six-electron oxidation of an aryl-amine precursor (NH2-CAM) to the aryl-nitro group of chloramphenicol (CAM). The ac...
4 downloads 10 Views 4MB Size
Subscriber access provided by UNIVERSITY OF ADELAIDE LIBRARIES

Article

CmlI N-Oxygenase Catalyzes the Final Three Steps in Chloramphenicol Biosynthesis without Dissociation of Intermediates Anna J. Komor, Brent S. Rivard, Ruixi Fan, Yisong Guo, Lawrence Que, and John D. Lipscomb Biochemistry, Just Accepted Manuscript • DOI: 10.1021/acs.biochem.7b00695 • Publication Date (Web): 20 Aug 2017 Downloaded from http://pubs.acs.org on August 21, 2017

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

Biochemistry is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

CmlI N-Oxygenase Catalyzes the Final Three Steps in Chloramphenicol Biosynthesis without Dissociation of Intermediates Anna J. Komor, †,¶ Brent S. Rivard, ,¶ Ruixi Fan,§ Yisong Guo,§ Lawrence Que, Jr.,†,¶ and John D. Lipscomb,¶,*



Department of Chemistry, Department of Biochemistry, Molecular Biology, and Biophysics,

and ¶Center for Metals in Biocatalysis University of Minnesota, Minneapolis, Minnesota 55455, United States §

Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA 15213, United States

1 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 2 of 50

ABSTRACT: CmlI catalyzes the 6-electron oxidation of an aryl-amine precursor (NH2-CAM) to the aryl-nitro group of chloramphenicol (CAM). The active site of CmlI contains a (hydr)oxo- and carboxylate-bridged dinuclear iron cluster. During catalysis, a novel diferric-peroxo intermediate P is formed and is thought to directly effect oxygenase chemistry. Peroxo intermediates can facilitate at most 2-electron oxidations, so the biosynthetic pathway of CmlI must involve at least 3 steps. Here, kinetic techniques are used to characterize the rate and/or dissociation constants for each step by taking advantage of the remarkable stability of P in the absence of substrates (decay t1/2 = 3 h at 4 °C) and the visible chromophore of the diiron cluster. It is found that diferrous CmlI (CmlIred) can react with NH2CAM and O2 in either order to form a P-NH2-CAM intermediate. P-NH2-CAM undergoes rapid oxygen transfer to form a diferric CmlI (CmlIox) complex with the aryl-hydroxylamine (NH(OH)-CAM) pathway intermediate. CmlIox-NH(OH)-CAM undergoes a rapid internal redox reaction to form CmlIred -nitrosoCAM (NO-CAM) complex. O2 binding results in formation of P-NO-CAM that converts to CmlIox-CAM by enzyme-mediated oxygen atom transfer. The kinetic analysis indicates that there is little dissociation of pathway intermediates as the reaction progresses. Reactions initiated by adding pathway intermediates from solution occur much more slowly than those in which the intermediate is generated in the active site as part of the catalytic process. Thus, CmlI is able to preserve efficiency and specificity while avoiding adventitious chemistry by carrying out the entire 6-electron oxidation in one active site.

2 ACS Paragon Plus Environment

Page 3 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

Introduction The final steps in the biosynthesis of chloramphenicol (CAM, Figure 1) by Streptomyces venezuelae are catalyzed by the N-oxygenase CmlI.1, 2 The substrate for CmlI is the aryl-amine analog of CAM (D-threo-1-(4-aminophenyl)-2-dichloroacetylamino-1,3-propanediol or NH2CAM), which undergoes a 6-electron oxidation, including two oxygenation steps, to yield the aryl-nitro group of the active antibiotic (Figure 1). Spectroscopic studies and the X-ray crystal structure of CmlI have shown that it has a (hydr)oxo and carboxylate-bridged dinuclear iron cluster in the active site.2, 3 Structurally similar clusters are found in many enzymes that activate O2 and then catalyze reactions such as functionalization of unactivated C-H bonds, desaturation reactions, aromatic hydroxylation, and radical formation, but notably, not aryl-amine oxygenation. 4-14 Conversely, CmlI and its structural and function homolog AurF15-19 do not catalyze the types of reactions common to other diiron oxygenases. Kinetic and spectroscopic studies of CmlI and AurF have shown that, despite the structural similarities to other diiron oxygenases, a different type of reactive oxygen intermediate is generated during catalysis. Both N-oxygenase enzymes generate long-lived peroxo intermediates that react directly with substrates,2, 18 as opposed to the high-valent oxo intermediates often formed by the other types of diiron oxygen-activating enzymes. 5, 20, 21 In CmlI, the peroxo intermediate (P) is exceptionally stable (decay t1/2 = 3 h at 4 °C and pH 9) when generated by adding O2 to the diferrous enzyme (Cmlred) in the absence of substrates.2 When P is mixed with aryl-amine substrates, it reacts in milliseconds to yield oxygenated products. The stability of P greatly facilitates transient kinetic experiments designed to investigate the kinetics of its reactivity with substrates. In recent studies, we have shown that it will react with the likely intermediates of the chloramphenicol

3 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 4 of 50

biosynthetic pathway including aryl-nitroso-CAM (NO-CAM), which has different electronic properties than NH2-CAM, demonstrating the catalytic diversity of P.22 Spectroscopic studies have also shown that P has a significantly different peroxo-bridging structure from the bridging cis-µ-1,2-peroxo structure found for almost all other characterized diiron-peroxo intermediates.2, 23

Peroxo intermediates, like the high-valent iron-oxo intermediates of other diiron oxygenases,5, 21, 24, 25 can carry out at most a 2-electron oxidation reaction, and thus the biosynthetic pathway of CmlI must have at least 3 steps. Studies of both CmlI and AurF 19, 22 have defined mechanistic proposals that differ substantially from the most straightforward scheme of simply repeating the oxygenation reaction of P three times with three pathway intermediates, a process that would require 6 external electrons.16, 26 The iteration of this mechanism that we have proposed for CmlI is shown in Figure 1. 22, 23 In this scheme, P is formed and reacted with NH2-CAM to make diferric CmlI (CmlIox) and an aryl-hydroxylaminoCAM (NH(OH)-CAM) intermediate. The resulting CmlIox-NH(OH)-CAM complex undergoes an internal redox reaction to yield Cmlred-NO-CAM which can bind O2 to reform P as a P-NOCAM complex. The final oxygenation reaction by this complex yields CAM and Cmlox. The internal reduction step means that this mechanism only requires 2 external electrons that are used to form the first P. This mechanism is supported by stepwise product formation studies showing the generation and reactivity of the predicted intermediates.22 Also, it has been observed that forming P with one isotope of O2 and then carrying out the reaction in a vessel with a different isotope of O2 in the headspace results in a mixed isotope nitro-group in CAM, thereby demonstrating reformation of P in the biosynthetic pathway. 22

4 ACS Paragon Plus Environment

Page 5 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

In the studies reported here, the dynamics of the predicted reaction pathway of CmlI are studied using transient kinetic techniques to determine rate and/or dissociation constants for each step in the process. In this way, the main tenets of the mechanism including the internal reduction step and the reaction of P with the chemically distinct substituent groups of the pathway intermediates can be independently demonstrated and quantified. In the course of this study, more subtle aspects of the process have also come to light including the mechanism by which the enzyme catalyzes the multistep reaction without loss of intermediates and with perfect specificity.

Figure 1. Proposed mechanistic cycle for N-oxygenation by CmlI.22, 23 Diiron cluster reduction steps are shown with red arrows. Color coding of the oxygen atoms highlights the fact that oxygen atoms from two different O2 molecules are incorporated into the final product. R = 2-dichloroacetylamino-1,3-propanediol.

Experimental Procedures Standard materials and procedures are described in the Supporting Information. The Dthreo-1-(4-aminophenyl)-2-dichloroacetylamino-1,3-propanediol (NH2-CAM) substrate was obtained from Toronto Research Chemicals, Toronto, CA. The NH(OH)-CAM and NO-CAM substrates were synthesized as previously described. 22

5 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 6 of 50

Stopped-Flow Analysis of P Formation and Single-Turnover Reactions. Stopped-flow reactions were performed using an Applied Photophysics model SX.18MV stopped-flow device configured for single wavelength collection at 300 nm (P formation reaction), 390 nm (reactions with NH(OH)-CAM) or 480 nm (reactions with NH2-CAM or NOCAM). All reactions were performed in 50 mM Bicine pH 9 at 4 °C. CmlI is fully functional between pH 6 and 9, but the stability of P is greatly enhanced at high pH. Consequently, it is possible to initiate transient kinetic experiments with CmlI in nearly a single form pH 9, simplifying the setup of experiments and the data analysis. The stopped-flow instrument was made anaerobic by flushing with dithionite solution followed by anaerobic buffer. CmlI was reduced as described in the Supporting Information and rapidly mixed with buffer containing varying concentration of O2 and substrate using the stopped-flow instrument (see figure legends). In some cases, substrate was added anaerobically to the diferrous CmlI (CmlIred) solution before mixing with O2-containing buffer. In cases where the P was preformed, it was generated by rapid mixture with an equivalent volume of O2-saturated buffer (or in some cases, buffer containing 0.9 equivalents of O2) in the gas tight syringe. In the reactions with NH(OH)-CAM, CmlI was not reduced, but was made anaerobic before the reaction was performed. Methods for analyzing reaction kinetics in order to determine rate constants and or dissociation constants are described in Supporting Information. These methods include procedures for fitting the time course to multiexponential equations and concentration dependencies to hyperbolic expressions. Mössbauer Analysis of the Reaction of CmlIred with O2 and NO-CAM. Mössbauer samples were prepared using an Update 715 ram syringe controller to mix solutions and dispense the mixtures onto counter-rotating aluminum wheels cooled with liquid nitrogen.27,

6 ACS Paragon Plus Environment

Page 7 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

28

The time between mixing and freezing was controlled using a calibrated set of delay tubing

between the mixer and a nozzle over the wheels. The counter rotating wheels grind the frozen solution into a powder which is deposited into the liquid nitrogen bath below the wheels. It is then collected and packed into a Mössbauer cup. In the experiments described here, one syringe held 1.25 mM CmlIred in 50 mM Bicine, pH 9, and the other held O2-saturated buffer with 6.25 mM NO-CAM. Time points collected were 20 ms, 80 ms, 250 ms, and 30 s. The Mössbauer spectra were analyzed as described in the Supporting Information.

Results P Formation Reaction. The P diferric peroxo intermediate of CmlI forms in less than one second when chemically reduced diferrous CmlI (CmlIred) is combined with O2. P is highly stable in the absence of substrate, exhibiting a t1/2 ~ 3 h at 4 °C and pH 9,2 and thus the formation reaction is expected to be irreversible. To determine the rate constant(s) for P formation, anaerobic CmlIred was mixed with 5-36 equivalents of O2 using a stopped-flow UV-vis instrument. The formation of P was followed at 300 nm, the wavelength where optical feature changes due to P formation are maximized (see Figure S1 for rationalization of wavelength choice here and in reactions described below). The resulting traces are best fit by a threesummed-exponential expression (Figure 2). Complete description of the techniques used for the analysis of transient kinetic data presented in this study can be found in the Supplemental Information. Plotting the reciprocal relaxations times (1/ or RRT) versus O2 concentration shows that all three phases have a linear dependence on O2 concentration with apparent secondorder rate constants of 58.1 ± 2.0, 19.6 ± 0.4, and 1.4 ± 0.1 s-1 mM-1 (Figure 3). The magnitude

7 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 8 of 50

of the total amplitude change stays the same over the range of O2 concentrations tested, and the three observed phases are approximately equal in amplitude.

Figure 2. Optical changes correlated with the formation of P by combining 40 μM CmlIred with 450 μM O2 in buffer (final, post-mix concentrations). Single- (blue), double- (green), and triple- (red) exponential fits of the P formation process shown by the black trace. Fit residuals are shown below the trace and highlight the need for a three exponential fit. 50 mM Bicine pH 9, 4 °C.

The presence of three phases linearly dependent on substrate is most easily accounted for by three parallel reactions to form P, rather than a single P formation process that employs three consecutive steps, which would yield nonlinear or no concentration dependence in two of the three phases. The Mössbauer spectrum of P shows only one type of cluster.2 If there are multiple Mössbauer-indistinguishable forms of P, they all appear to react with substrates (see below). The multiple phase P formation behavior is likely to be the result of either or both of the following scenarios: (a) three different pathways for O2 binding that all lead to the same P, or (b) the existence of CmlIred in three different structural or protonation states that differentially affect P formation. While the Mössbauer spectra of CmlIred show only a single species, the spectra of CmlIox reveal that several forms exist in a pH dependent distribution.2 The concentration dependence plots of all phases have a y-intercept close to zero, showing that the formation of P 8 ACS Paragon Plus Environment

Page 9 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

in the absence of substrate is nearly irreversible, as expected. This finding is also in accord with our previous demonstration that P does not exchange with head space O2 over the course of hours.22

Figure 3. O2 concentration dependence of P formation. 40 µM CmlIred (final, post mix concentration) was mixed in a 1:1 ratio with varying concentrations of O2 in buffer. RRT-1, -2, and -3 (■,●,▲, respectively) from multiexponential fitting of stopped-flow traces are plotted versus O2 concentration, all showing linear relationships. The second order rate constant for each process was determined from the slope of the linear fit to the data (solid line), and they are reported in the text. Reported error of each point is one standard deviation from the mean. 50 mM Bicine pH 9, 4 °C.

Kinetic Parameters of the Reaction of P with NH2-CAM. The next step of the CmlI cycle that can be isolated is the reaction of P with NH2-CAM to form NH(OH)-CAM and CmlIox, followed by oxidation of NH(OH)-CAM to NO-CAM and reduction of the diferric cluster to form CmlIred. In order to explore this reaction, P was formed with 0.9 equivalent of O2 (to ensure no excess O2 in the reaction) and then loaded immediately on the stopped-flow instrument for reaction with 5-40 equivalents of NH2-CAM dissolved in anaerobic buffer. When monitored at 480 nm, both P decay and the subsequent reduction of the diiron cluster appear as a decrease in absorbance. Both processes are first order or pseudo-first order, and the reaction halts after the last step, so summed exponential fitting is appropriate (see Supporting Information for additional details).

9 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 10 of 50

The time courses are fit well by a two-summed-exponential expression (Figure 4A). Both exponentials have positive amplitudes (a positive amplitude sign correlates with decreasing absorbance), and the phase with larger RRT contributes ~85% of the total absorbance change. Since the types of reactions involved are effectively irreversible (O-O bond cleavage and 100% diiron cluster reduction, see below), it is possible to assign the two RRTs to rate constants for two steps of the reaction. The simplest scenario for the reaction shown in Scheme 1A is to assign one RRT to the rate constant for conversion of P to CmlIox, and the second to the rate constant for reduction of CmlIox to CmlIred. However, analysis of the absorbance changes makes this scenario unlikely. The expected absorbance due to P, CmlIox, and CmlIred at 480 nm at various stages of the reaction can be determined using the extinction coefficients of the species (Table S1) and the concentration of CmlI in the experiment (there is negligible absorption due to any of the organic CAM substrates at 480 nm). The starting sample (Abs. = 0.11, Figure 4B, orange dashed line) was prepared to have 10% CmlIred and 90% P. The first step in the proposed mechanistic model is the conversion of P and NH2-CAM to CmlIox and NH(OH)-CAM. The corresponding predicted absorbance of 90% CmlIox and the remaining 10% CmlIred would give Abs = 0.072 (Figure 4B, blue dashed line). After re-reduction of the CmlI by NH(OH)-CAM formed in situ, the endpoint pure CmlIred spectrum would give Abs = 0.046 (Figure 4B, black dashed line). Consequently, approximately equal changes in absorbance should result from each step. The observation that the rapid segment of the time course results in an absorbance significantly below the blue dashed line shows that more than just the P conversion to CmlIox has occurred during the fast phase.

10 ACS Paragon Plus Environment

Page 11 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

An alternative interpretation for the overall 2-phase fit of the time course with unequal amplitudes illustrated in Scheme 1B is that there are two independent processes starting from two different forms of P in an 85:15 ratio (based on the observed ratio of fast and slow phase amplitudes). If the reduction step following the reaction of the dominant form of P with NH2CAM is much faster (> 5 fold), the reaction will appear as a single exponential time course proceeding below the absorbance demarcated by the blue dashed line. Thus, the dominant phase would be reflective of both P decay and the fast reduction. The second observed phase would then describe a smaller fraction of P reacting similarly, but with a lower initial rate constant.

11 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 12 of 50

Figure 4. Optical changes at 480 nm correlated with the reaction of 180 µM P with 2 mM NH2-CAM. A: single(blue trace) and double- (red trace) exponential fits of the substrate-mediated P decay process (black trace). Fit residuals are shown below the trace. B: Reaction as in A. Dashed lines indicate the calculated absorbance of 180 µM P + 20 µM CmlIred, 180 µM CmlIox + 20 µM CmlIred, and 200 µM CmlIred. 50 mM Bicine pH 9, 4 °C.

Scheme 1. Proposed Schemes for the Reaction of P with NH2-CAMa

a

Rate constants are derived from the plots in Figure 5. For simplicity CmlIox and CmlIred are abbreviated as Eox and Ered, respectively. P’ and E’ represent CmlI species that are kinetically distinct from P and E. A: represents the case in which there is a single reaction pathway for P reacting with NH2-CAM. B: represents the case in which two parallel pathways are possible beginning from two forms of P.

The selection of Scheme 1B over 1A is also supported by plots of the RRTs from each exponential phase versus the concentration of NH2-CAM (Figure 5). The resulting plots are hyperbolic, suggesting that an unobserved, fast, reversible second-order NH2-CAM binding process precedes P decay (see Supporting Information, Methods). The dissociation constants for complex formation reactions for the faster and slower processes are KD = 8.5 ± 1.5 mM and KD = 3.6 ± 1 mM, respectively. Analysis of the hyperbolic curves (see Figure 5A and Supplemental Information) show that the rate constants for the step following binding are kf = 79.6 ± 5 s-1 and kr ≈ 0 s-1 for the faster process and kf = 0.9 ± 0.1 s-1 and kr ≈ 0 for the slower process. The irreversible nature of the reaction is reasonable considering that it involves the cleavage of an OO bond and insertion of an O atom into an N-H bond as P reacts with NH2-CAM. If the reaction is irreversible, then in Scheme 1A, the concentration dependence on NH2-CAM will be lost in the second phase, which is not the case. Moreover, it is shown below that modeling the time 12 ACS Paragon Plus Environment

Page 13 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

course of the complete biosynthetic pathway requires a reduction step with a rate constant 2-3 orders of magnitude greater than that shown in Scheme 1A.

Figure 5. NH2-CAM concentration dependence of the RRTs for the reaction of P with NH2-CAM. Extracted RRTs plotted versus [NH2-CAM] for the reaction of P (180 µM, final post-mix concentration) with varying concentrations of NH2-CAM in anaerobic buffer. The generic method for analysis is illustrated in panel A where E and E’ are two forms of the enzyme and S is a substrate and S’ is a modified form of S (See Supporting Information). A: RRT-1, hyperbolic fit gives KD = 8.5 ± 1.5 mM, kf = 79.6 ± 5 s-1, and kr ≈ 0 s-1. B: RRT-2, hyperbolic fit gives KD = 3.6 ± 1 mM, kf = 0.9 ± 0.1 s-1, and kr ≈ 0 s-1. 50 mM Bicine pH 9, 4 °C.

Reaction of CmlIox with NH(OH)-CAM. The reduction of CmlIox by NH(OH)-CAM can also be monitored by simply mixing these two reactants anaerobically. Careful scrubbing of O2 from the reaction buffers and the stopped-flow instrument ensures that the reaction stops after the reduction process and does not proceed to reform P for the final oxidation step. In order to study this step, CmlIox was made anaerobic and then mixed in a 1:1 ratio with anaerobic buffer 13 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 14 of 50

containing varying concentrations of NH(OH)-CAM, all of which were appropriate to establish pseudo first order conditions. The resulting optical change at 390 nm was a decrease in absorbance; the time course trace fit to a double summed-exponential equation (Figure 6). The monitoring wavelength was chosen to maximize optical change while minimizing the contribution of the NH(OH)-CAM that occurs at lower wavelengths. The net absorbance change of ~0.03 matched the expected absorbance change for the conversion of 40 μM CmlIox to CmlIred.

Figure 6. Optical change at 390 nm upon the anaerobic mix of 40 µM CmlIox and 2 mM NH(OH)-CAM (final, postmix concentrations). The trace fits best to a two exponential equation, as shown by the colored fit lines and the residuals for 1- (blue) and 2- (red) exponential fits shown below the trace. 50 mM Bicine pH 9, 4 °C.

The plots of RRT-1 and RRT-2 versus NH(OH)-CAM concentration are both hyperbolic (Figure 7), suggesting that a relatively fast step, presumably NH(OH)-CAM binding (KD = 1.1 mM), precedes the CmlI reduction occurring in the observable steps. The rate constants extracted from these plots (RRT-1: kf = 1.3 ± 0.1 s-1 and kr ≈ 0 and RRT-2: kf = 0.23 ± 0.03 s-1, kr ≈ 0) are very slow compared with the rate constant for reduction of the diiron cluster observed when

14 ACS Paragon Plus Environment

Page 15 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

starting the reaction with NH2-CAM as described above. The slower phase disappears as the concentration of NH(OH)-CAM increases, suggesting that the biphasic kinetics arise from some sort of allosteric effect of substrate that will not be pursued further here. A model for the reaction of CmlIox and NH(OH)-CAM is shown in Scheme 2. Scheme 2. Proposed Scheme for the Reaction of CmlIox with NH(OH)-CAMa

a For simplicity CmlIox and CmlIred are abbreviated as Eox and Ered, respectively. The intermediate Eox-NH(OH)CAM’ and the assignment of the rate constant for the reduction step as “fast” are proposed based on modeling of the overall biosynthetic reaction pathway kinetics (see Discussion, Simulation of the Overall Reaction).

The results indicate that the reduction of the diiron cluster by NH(OH)-CAM occurs much faster when this pathway intermediate is generated in situ in the active site rather than having to bind from solution. Moreover, if NH(OH)-CAM dissociates from the active site after it is generated, but before it can reduce the diiron cluster, the subsequent reduction step would presumably occur with the slow rate constants observed for the reaction of NH(OH)-CAM in solution with CmlIox. This route for cluster reduction should thus be considered an off-pathway process.

15 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 16 of 50

Figure 7. NH(OH)-CAM concentration dependence of the RRTs for the reaction of 40 µM anaerobic CmlIox (final, post mix-concentration) and varying concentrations of NH(OH)-CAM in anaerobic buffer. ■: Hyperbolic fits of RRT-1s extracted from the traces of the reaction, giving KD = 1.1 ± 0.05 mM, kf = 1.3 ± 0.1 s-1 and kr ≈ 0. ●: Hyperbolic fits of RRT-2s extracted from the traces of the reaction, giving KD = 1.2 ± 0.3 mM, kf = 0.23 ± 0.03 s-1 and kr ≈ 0. RRT-2 is not observed above 8 mM NH(OH)-CAM. 50 mM Bicine pH 9, 4 °C.

Reaction of P with NO-CAM. Anaerobic P was formed as described above and mixed with NO-CAM dissolved in anaerobic buffer. Surprisingly, little to no reaction was observed when monitored at 480 nm (Figure S2). Alternative ways to approach this reaction allow the kinetic time course to be monitored and the observation of product as described below. Reaction of CmlIred with NO-CAM and O2. The reaction in which NO-CAM is converted to CAM can be examined by mixing CmlIred with a buffer solution containing 5-150 fold excess of NO-CAM and a 5-fold excess O2 (a saturated solution) (Figure 8A). At 480 nm, one would expect to observe an increase in absorbance as P is formed and then a decrease as the NO-CAM is converted to CAM with the formation of CmlIox. Conducting the reaction in this way gave time courses that are fit well by a three-summed exponential equation. The resulting RRTs were plotted versus NO-CAM concentration as shown in Figure 8B. The faster two phases show a hyperbolic dependence on NO-CAM concentration, while the slowest phase shows no dependence. In this case, the amplitudes of the two faster phases have opposite signs, making it unlikely that they arise from parallel reactions. The hyperbolic dependences indicate that there is a fast, reversible step that precedes the observable reaction, which must itself consist of at least 3 additional steps in accord with the three-summed-exponential fit.

16 ACS Paragon Plus Environment

Page 17 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

Figure 8. Reaction of CmlIred with NO-CAM in O2-saturated buffer. A: Optical changes at 480 nm upon mixing 200 µM CmlIred with buffer containing 2 mM NO-CAM and 0.9 mM O2 (all post mix, final concentrations). A threeexponential fit (red line) best simulates the time course and is shown superimposed on the data (black line). Residuals for two- (blue line) and three- (red line) exponential fits are shown below the data. B: Fits of the RRTs versus NO-CAM concentration. Black: RRT-1 hyperbolic fit, kf = 150.4 ± 8.8 s-1 mM-1 (at 0.9 mM O2), kr = 19.4 ± 2 s-1, KD-binding = 8.6 ± 1 mM, KD-observed step = 0.13 mM. Blue: RRT-2 hyperbolic fit, kf = 37.7 ± 5 s-1, kr ~ 0 s-1. Red: RRT-3 linear fit, estimate of concentration-independent rate constant, kf + kr’ = 5.2 ± 0.1 s-1. Error range for the blue and red points are within the size of the symbol. 50 mM Bicine pH 9, 4 °C.

Although the observed kinetics of the reaction of CmlIred with O2 and NO-CAM would support a variety of 4-step processes which include a binding step, Scheme 3 shows one possibility that is reasonable based on the chemistry of the biosynthetic pathway. In this model, NO-CAM binding is the fast reversible step that precedes the optically observable steps with KD = 8.6 ± 1 mM. Reversible (Figure 9, black curve, non-zero y-intercept) O2 binding occurs in the 17 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 18 of 50

following step to form P, giving a fast increase in absorbance. The reversible nature of this step would be expected to yield non-linear plot for another RRT, as observed. In the Scheme 3 model, the P reacts in the subsequent step with NO-CAM irreversibly to give a decrease in absorbance. The presence of two reversible steps in the 3 step series to this point (beginning with binding) should, in principle, be analyzed using the roots of a cubic equation. However, the large difference in the observed maximum RRTs allows the rate constants for the individual steps to be approximated from the maximum (kf’ + kr) and intercept (kr) of the two hyperbolic plots. This approximation gives kf = 150.4 s-1 mM-1 (at 0.9 mM O2) and kr = 19.4 s-1 for O2 binding (KD = 0.13 mM) to form P and kf = 37.7 s-1 and kr = 0 for the P reaction with bound NO-CAM. The irreversible nature of the latter step (zero intercept for the plot in Figure 8B, blue curve) uncouples the third RRTs from NO-CAMs concentration, so the final concentration-independent step occurs with kf + kr’ = 5.2 s-1 (Figure 8B, red curve). This step is likely to be product release and represent the rate constant limiting substrate flux through the cycle. The small amplitude of this slow phase (< 10% those of the faster phases) is consistent with the very small change in absorbance at 480 nm caused by the binding of CAM to CmlIox.22 At high NO-CAM concentrations, the faster RRT reaches values that far exceed the expected values based on the rate constant for P formation in the absence of NO-CAM (see Figure 3 above). This suggests that in the NO-CAM complex, O2 binding is facilitated, allowing much faster P formation. It also suggests that NO-CAM binding precedes O2 binding, consistent with the increasing maximum value of P formed as the concentration of NO-CAM increases (Figure 9). Any P that forms prior to NO-CAM binding would yield a dead-end complex, as the results presented above and in Figure S2 show that P does not react with NO-CAM. Since there

18 ACS Paragon Plus Environment

Page 19 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

is no substantial buildup of P at the end of the reaction, it is likely that NO-CAM binding is very fast.

Scheme 3. Proposed Scheme for the Reaction of CmlIred with NO-CAMa

a

For simplicity CmlIox and CmlIred are abbreviated as Eox and Ered, respectively.

Figure 9. NO-CAM concentration dependence of the time course of the reaction of CmlIred with pseudo-first order concentrations of O2 and NO-CAM. The traces follow the reaction of 200 µM CmlIred with 1-30 mM NO-CAM in O2-saturated buffer, 50 mM Bicine pH 9, 4 °C.

Verification of P as the Active Oxidant that Acts on NO-CAM. One possible explanation for the failure of preformed P to react with NO-CAM is that a different form of P is made when NO-CAM is present in active site. To examine this possibility, short time point

19 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 20 of 50

samples of the reaction of CmlIred with an excess of NO-CAM and O2 were prepared by a rapidfreeze quench procedure and analyzed by Mössbauer spectroscopy (Figure 10, top).

Figure 10. Top: Time points of RFQ samples for Mössbauer analysis of the reaction of 200 µM CmlIred with 0.9 mM O2 and 2 mM NO-CAM (final, post mix concentrations). Inset table shows the fraction of the sample present as P quantified from the Mössbauer spectra. Bottom: Mössbauer spectra of the samples. The black lines are the experimental data and the colored lines are fits to various species: diferrous (blue), intermediate P (red) and resting state diferric (green). A small fraction of mononuclear ferric ion also appears at the end point. 50 mM Bicine pH 9, 4 °C.

Mössbauer analysis (Figure 10, bottom) showed a decrease in CmlIred over the course of the reaction, concomitant with an increase in P. The spectral parameters for P formed in this way are the same as those for P formed in the absence of substrate.2 P rises to a maximum and decays 20 ACS Paragon Plus Environment

Page 21 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

following approximately the time course of the 480 nm species observed in the reaction of NOCAM with CmlIred and O2 (Figure 9). At long time (30 s), < 5% P is present and the sample is predominantly diferric. Previous experiments have shown that CAM is formed in this reaction.22 Thus, Mössbauer analysis suggests that intermediate P formed in the presence or absence of substrate has identical Mössbauer parameters, and is the oxidant that acts on NO-CAM prebound in the active site. Kinetic Parameters of the Complete Reaction Pathway. The complete biosynthetic pathway was examined in two ways: (a) by pre-equilibrating NH2-CAM anaerobically with CmlIred to allow the complex to reach equilibrium and then initiating the reaction by mixing with O2-saturated buffer, or (b) by mixing CmlIred with O2-saturated buffer containing various concentrations of NH2-CAM. No significant difference in trends or magnitudes of RRTs was observed between the two iterations. The data presented is for the latter combination. All optical changes were observed by stopped-flow UV-vis spectroscopy at 480 nm and 4 °C, pH 9. This wavelength was chosen because it gives the maximum optical change for both the P formation and P decay processes. Using a shorter wavelength gives a greater optical change for P formation, but P decay is masked by reappearance of the Fe-O-Fe charge transfer band of diferric CmlI, which has a shoulder at ~375 nm. Initiating the reaction in this way allows both P formation and substrate-mediated P decay to be observed (Figure 11). After P forms and decays, the resulting CmlIox is reduced by the NH(OH)-CAM product of the first reaction to give a further decrease in absorbance. This reduction is followed by binding of O2 to reform P, resulting in an increase in absorbance. Finally, P decays as CAM is formed to give a decrease in absorbance.

21 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 22 of 50

Figure 11. NH2-CAM concentration dependence of the overall reaction time course. Solid curves: Optical changes at 480 nm from the reaction of CmlIred (200 µM) with 1-16 mM NH2-CAM (final, post mix concentrations) in O2saturated buffer. Dashed curves: Simulation of the same reaction using numerical integration. The rate constants and reactions used for the simulation are shown in Scheme 4 (see Discussion). Post-mix [O2] ~ 0.9 mM at 4 °C. 50 mM Bicine pH 9, 4 °C.

In sharp contrast to the trend shown above for the reaction of CmlIred with O2 and NOCAM, the maximum amount of P formed decreases with increasing substrate concentration when NH2-CAM is the substrate. This suggests that the two reactions proceed differently. The traces in Figure 11 show that as the concentration of NH2-CAM increases, the pseudo first order rate constants for P formation and decay converge. Unfortunately, this convergence makes the resolution of the RRTs by summed-exponential fitting unreliable. Some insight into this complex overall reaction and the differences in P reactivity at different steps can be gained by combining the measured kinetic and thermodynamic parameters for each step with numerical integration of the overall reaction. This approach to the analysis is explored in the Discussion.

Discussion The results presented here show that the complex reaction pathway for the final steps in the biosynthesis of chloramphenicol can be studied in segments to extract rate constants and/or thermodynamic parameters for each step. The major tenets of the proposed reaction cycle shown 22 ACS Paragon Plus Environment

Page 23 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

in Figure 1 are supported by these studies. In particular, the data demonstrates the oxygenase reactivity of the peroxo intermediate P with NH2-CAM and NO-CAM as well as the ability of the pathway intermediate NH(OH)-CAM to reduce the CmlI diferric cluster in preparation for the proposed mid-pathway reformation of P. The results also reveal several new aspects of the pathway and its regulation, including insight into the effect of substrate binding on the rate constant for O2 binding and the dramatic difference in the rate constant for cluster reduction by NH(OH)-CAM formed in situ versus that binding from solution. Kinetic evidence is found for progress along the biosynthetic pathway at rates which are large compared with dissociation of intermediates from the enzyme, providing insight into how the enzyme efficiently accelerates catalysis while maintaining specificity. These new aspects of CmlI catalysis are discussed here.

Regulation of P Formation Rate and Substrate Binding Order. The set of time courses shown in Figure 11 represent the overall biosynthetic process beginning with NH2-CAM and O2 binding to CmlIred. The time courses look similar when NH2-CAM is preincubated with CmlIred before mixing with O2. It is evident that this process differs in two respects from that later in the pathway in which CmlIred reacts with NO-CAM and O2. First, the NO-CAM reaction has a strict binding order such that pre-incubation with O2 to form P stops the reaction (Figure S2). Second, the maximal amount of P formed and the apparent rate at which it is formed increase with increasing NO-CAM concentration (Figure 9), but decrease with increasing NH2CAM concentration (Figure 11). This observation is readily rationalized in the case of NO-CAM because the CmlIred-NO-CAM complex must form first in order to allow P formation in a way that can go on to form CAM (Figure S2). In contrast, the rationale for the decreasing accumulation of P in the NH2-CAM reaction proposed in Scheme 4 is more complex. The lack

23 ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 24 of 50

of a preferred order of addition of substrates in this case suggests that it can proceed via two parallel routes. Experimental data are reported here for the rate constants and binding KD values for the route in which O2 can bind first (constants shown in black in Scheme 4) (Figures 3 and 5). The results show that in the absence of NH2-CAM, P forms by 3 kinetically distinguishable routes. However, as shown by the numerical integration fit to the data shown in Figure 11 (see below), when even low levels of NH2-CAM (or NO-CAM, see Figure 8 and Scheme 3) are present, only one rate constant for P formation is required to fit the time course. Interestingly, the observed rate constant is not the same as any found in the absence of a substrate. This finding suggests that substrate makes the CmlIred population homogeneous with respect to P formation while altering the rate of the process, by a mechanism that is currently not understood. The dissociation and rate constants for the branch of the pathway starting with NH2-CAM binding are more difficult to determine directly due to the lack of a spectral change upon NH2-CAM binding, the similarity of the rate constants for P formation and decay, and the inability to limit the reaction to a few steps. However, the presence of this alternative pathway is necessary to account for the decreasing maximal accumulation of P with increasing NH2-CAM. This observation is true because, at low concentrations of NH2-CAM, the initial O2 binding pathway is preferred and P decays slowly after it is formed due to the relatively low affinity of P for NH2-CAM (KD = 8.5 mM). Consequently, P maximally accumulates. As the NH2-CAM concentration increases, the rapid, high affinity NH2-CAM binding pathway is preferred leading efficiently to the P-NH2CAM intermediate, which is very rapidly converted to CmlIox-NH(OH)-CAM. Consequently, neither P nor the complex of P with a substrate accumulates.

24 ACS Paragon Plus Environment

Page 25 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

Scheme 4. Proposed Scheme for the Overall Reaction of CmlIred with NH2-CAM and O2 to Form CAMa

a

The proposed scheme synthesizes all the kinetic data collected in this study. The figure or scheme that first introduced each rate constant or KD value is indicated. For simplicity CmlIox and CmlIred are abbreviated as Eox and Ered, respectively. Bold black intermediate names and arrows represent components of the main pathway. Blue-green intermediate names and arrows are experimentally accessible components but are thought to be side pathways. The rate constants for intermediates leaving by the side pathways are slow and have little effect on the observed time course of the reaction. The rate constants and dissociation constants shown in black were determined experimentally in this work and are fixed in the numerical integration shown in Figure 11 (dashed curves). The rate constants and dissociation constants shown in red were determined by the numerical integration program to best fit the data over a range of substrate concentrations. b These constants can only be varied over a only a small (> 5%) range and still give a reasonable fit to the data. c This constant can assume any value >300 s-1. d These constants can only be varied over a large range and still give a reasonable fit to the data. e The dissociation of NO-CAM for this step must be 5%) range and still give a reasonable fit to the data.  cThis constant can assume any value >300 s-1.  dThese constants can only be varied over a large range and still give a reasonable fit to the data.  eThe dissociation of NO-CAM for this step must be < 1 s-1.   fThe KD refers to the binding reaction.  67x26mm (600 x 600 DPI)

ACS Paragon Plus Environment

Page 48 of 50

Page 49 of 50

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Biochemistry

Scheme 5. Model for CmlI Biosynthetic Pathway in One Active Site 42x21mm (600 x 600 DPI)

ACS Paragon Plus Environment

Biochemistry

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Table of Contents Graphic 33x16mm (600 x 600 DPI)

ACS Paragon Plus Environment

Page 50 of 50